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[病毒样颗粒疫苗以及HIV-1包膜蛋白修饰对其抗原特性的影响]

[VLP vaccines and effects of HIV-1 Env protein modifications on their antigenic properties].

作者信息

Vzorov A N, Compans R W

机构信息

Department of Microbiology and Immunology and Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA, 30322, USA.

Ivanovskii Institute of Virology, Gamaleya Federal Research Center for Epidemiology and Microbiology, Ministry of Healthcare of the Russian Federation, Moscow, 123098, Russia.

出版信息

Mol Biol (Mosk). 2016 May-Jun;50(3):406-15. doi: 10.7868/S0026898416030113.

Abstract

An ideal protective HIV-1 vaccine can elicit broadly neutralizing antibodies, capable of preventing HIV transmission. The strategies of designing vaccines include generation of soluble recombinant proteins which mimic the native Env complex and are able to enhance the immunogenicity of gp120. Recent data indicate that the cytoplasmic tail (CT) of the Env protein has multiple functions, which can affect the early steps of infection, as well as viral assembly and antigenic properties. Modifications in the CT can be used to induce conformational changes in functional regions of gp120 and to stabilize the trimeric structure, avoiding immune misdirection and induction of non-neutralizing antibody responses. Env-trimers with modified CTs in virus-like particles (VLPs) are able to induce antibodies with broad spectrum neutralizing activity and high avidity and have the potential for developing an effective vaccine against HIV.

摘要

一种理想的HIV-1保护性疫苗能够引发具有广泛中和能力的抗体,从而预防HIV传播。疫苗设计策略包括生成可溶性重组蛋白,这些蛋白模拟天然Env复合物并能够增强gp120的免疫原性。最近的数据表明,Env蛋白的胞质尾(CT)具有多种功能,可影响感染的早期步骤以及病毒组装和抗原特性。CT的修饰可用于诱导gp120功能区的构象变化并稳定三聚体结构,避免免疫误导和非中和抗体反应的诱导。病毒样颗粒(VLP)中具有修饰CT的Env三聚体能够诱导具有广谱中和活性和高亲和力的抗体,并且具有开发有效HIV疫苗的潜力。

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